A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497392



Internal ID20870598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67599301..67601700hg38UCSC Ensembl
chr15:67891639..67894038hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025466
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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